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Phenotypic Abnormality (PA): Clubbing

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of skeletal morphology [HP:0011842] <18>(87|89) (90|49|32)
+ + + + 4:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + + + 4:   Abnormality of the skeletal system [HP:0000924] <7>(89|98) (94|51|33)
+ + + 3:   Abnormality of limb bone [HP:0040068] <1>(28|30) (30|18|20)
+ + + 3:   Abnormal appendicular skeleton morphology [HP:0011844] <4>(35|41) (38|23|23)
+ + 2:   Abnormality of limb bone morphology [HP:0002813] <13>(28|30) (30|18|20)
+ 1:   Abnormal digit morphology [HP:0011297] <10>(16|19) (17|14|16)
0:   Clubbing [HP:0001217] <2>(0|1) (0|0|1)
- 1:   Clubbing of fingers [HP:0100759](0|0) (0|0|1)
- 1:   Clubbing of toes [HP:0100760](0|1) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
RecA protein-like (ATPase-domain)0.0005209Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
52540,52540,52540
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 52540 - P-loop containing nucleoside triphosphate hydrolases
  • 0.0007518Direct